Hand Sanitizer (Alcohol) Gel [Mckesson] -

HAND SANITIZER (ALCOHOL) GEL [MCKESSON]
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NDC	49348-405-31, 49348-405-37
Set ID	96bc1495-0633-4348-bfce-7ee2c4eaf04c
Category	HUMAN OTC DRUG LABEL
Packager	STRATEGIC SOURCING SERVICES LLC
Generic Name
Product Class
Product Number
Application Number	PART333A

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Active Ingredient

Ethyl alcohol 70%
Purpose

Antiseptic
Uses
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings

For external use only-hands

Flammable. Keep away from heat and flame.
When using this product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- avoid contact with broken skin
- do not inhale or ingest
Stop use and ask a doctor if

Skin irritation develops
Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center right away.
Directions
- wet hands thoroghly with product and allow to dry without wiping
- for children under 6, use only under adult supervision
- not recommended for infants
Other information
- do not sore above 105⁰ F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4
SPL UNCLASSIFIED SECTION

Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds*

Not manufactured or distributed by GOJO industries, Inc. distributor of Purell Refreshing Gel Advanced Hand Sanitizer**

Made in USA with US and foreign components

Another Quality Product Distributed By McKesson
One Post Street, San Francisco, CA 94104
Money Back Guarantee
Please visit us at www.sunmarkbrand.com

SDS-MO-15036 SDA-WI-2486 DSP-MO-28 DSP-MO-34
principal display panel

Sunmark

COMPARE TO PURELL**

NDC 49348-405-37

hand sanitizer

more effective formula

Kills more than 99.99% of germs*

ADVANCED

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49348-405
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
SULISOBENZONE (UNII: 1W6L629B4K)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49348-405-31	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/21/2013
2	NDC:49348-405-37	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/21/2013